Evidence map›Paper›PMID 41988200›Full record

ArticleFrontiers in immunology2026

The mechanism of PKM2/HIF-1α axis polarizing TAMs by upregulating glucose-serine metabolism to promote melanoma progression.

Ying Yang, Peng Su, Xinqi Yang, Na Liang, Xiang Huang, Ying Sun, Changxian Chen, Hua Chen, Chunming Li, Jiawei Yang and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Ying Yang *Department of Dermatology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Peng Su *Department of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Xinqi YangDepartment of Urology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Na LiangDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Xiang HuangDepartment of Urology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Ying SunDepartment of Dermatology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Changxian ChenDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Hua ChenDepartment of Dermatology, Jiangsu Provincial People's Hospital Chongqing Hospital, Chongqing, China.
Chunming LiDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Jiawei YangDepartment of Biochemistry, Zunyi Medical University, Zunyi, Guizhou, China.
Neng ZhangDepartment of Urology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Melanoma is the most aggressive skin cancer. Tumor-associated macrophages (TAMs) promote melanoma progression through polarization, however, whether glucose-serine metabolism regulates TAMs polarization and the specific regulatory mechanism remain unclear. Methods: Immunohistochemistry (IHC) was used to detect the infiltration of M2-type TAMs in melanoma tumor tissues; bioinformatics analysis was employed to identify HIF-1α, a key gene regulating glucose metabolism and polarization of TAMs; Results: M2-type TAMs were highly enriched in melanoma tumor tissues and closely associated with tumor progression and poor prognosis. Single-cell sequencing data of melanoma suggested that HIF-1α is a key gene regulating glucose metabolism and polarization in TAMs. Conclusions: Our study reveals that the PKM2/HIF-1α axis upregulates glucose-serine metabolism to induce M2 polarization of TAMs and drive melanoma progression. Targeting this metabolic axis thus holds promise as a novel therapeutic strategy for melanoma patients.

Indexed as

Carrier ProteinsGlucoseHypoxia-Inducible Factor 1, alpha SubunitMelanomaMembrane ProteinsSerineSkin NeoplasmsThyroid HormonesTumor-Associated MacrophagesAnimalsCell Line, TumorDisease ProgressionGene Expression Regulation, NeoplasticHumansMetabolic ReprogrammingMiceCarrier ProteinsGlucoseHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMembrane ProteinsSerineThyroid Hormone-Binding ProteinsThyroid Hormonesde novo serine synthesisglucose-serine metabolismHIF-1αmelanomaPKM2tumor-associated macrophages(TAMs)

Identifiers

PMID41988200
PMCPMC13076481

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.